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牛白血病病毒基因组中的新型单核苷酸多态性与前病毒载量相关,并影响病毒非编码转录本的表达谱。

Novel single nucleotide polymorphisms in the bovine leukemia virus genome are associated with proviral load and affect the expression profile of viral non-coding transcripts.

机构信息

National Institute of Animal Health, National Agriculture and Food Research Organization, 3-1-5 Kannondai, Tsukuba, Ibaraki, 305-0856, Japan.

Kenhoku Livestock Hygiene Service Center, Ibaraki Prefecture, 966-1 Nakagachi, Mito, Ibaraki, 310-0002, Japan.

出版信息

Vet Microbiol. 2021 Oct;261:109200. doi: 10.1016/j.vetmic.2021.109200. Epub 2021 Aug 5.

Abstract

Bovine leukemia virus (BLV) infects bovine B-cells and causes malignant lymphoma, resulting in severe economic losses in the livestock industry. To control the spread of BLV, several studies have attempted to clarify the molecular mechanisms of BLV pathogenesis, but the details of the mechanism are still enigmatic. Currently, viral non-coding RNAs are attracting attention as a novel player for BLV pathogenesis because these transcripts can evade the host immune response and are persistently expressed in latent infection. One of the viral non-coding RNA, AS1, is encoded in the antisense strand of the BLV genome and consists of two isoforms, AS1-L and AS1-S. Although the function of the AS1 is still unknown, the AS1 RNA might also have some roles because it keeps expressing in tumor tissues. In the present study, we identified novel single nucleotide polymorphisms (SNPs) located in the AS1 coding region and indicated that individuals infected with BLV with minor SNPs showed low proviral load. To evaluate the effect of identified SNPs, we constructed infectious clones with these SNPs and found that their introduction affected the expression profile of AS1 RNA; the amount of AS1-L isoform increased compared with the wild type, although the total amount of AS1 RNA remained unchanged. Prediction analysis also suggested that the introduction of SNPs changed the secondary structure of AS1 RNA. These results explain part of the relationship between BLV expansion in vivo and the expression profile of AS1, although further analysis is required.

摘要

牛白血病病毒(BLV)感染牛 B 细胞并导致恶性淋巴瘤,给畜牧业造成严重的经济损失。为了控制 BLV 的传播,已有多项研究试图阐明 BLV 发病机制的分子机制,但该机制的细节仍不清楚。目前,病毒非编码 RNA 作为 BLV 发病机制的新参与者引起了关注,因为这些转录本可以逃避宿主的免疫反应,并在潜伏感染中持续表达。病毒非编码 RNA 之一 AS1 是 BLV 基因组反义链上编码的,由两个亚型 AS1-L 和 AS1-S 组成。虽然 AS1 的功能仍不清楚,但 AS1 RNA 也可能具有一些作用,因为它在肿瘤组织中持续表达。在本研究中,我们鉴定了位于 AS1 编码区的新的单核苷酸多态性(SNP),并表明感染 BLV 的个体中存在 minor SNPs 时,前病毒载量较低。为了评估鉴定的 SNPs 的影响,我们构建了带有这些 SNPs 的感染性克隆,并发现它们的引入影响了 AS1 RNA 的表达谱;与野生型相比,AS1-L 亚型的数量增加,尽管 AS1 RNA 的总量保持不变。预测分析还表明,SNP 的引入改变了 AS1 RNA 的二级结构。这些结果解释了 BLV 在体内扩增与 AS1 表达谱之间的部分关系,但仍需要进一步分析。

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